Question

excess AICl3 Cl︿Cl phosgene

ketone products can be efficiently constructed by sequential Friedal-Crafts acylations with phosgene.
a- draw an arrow pushing mechanism for the double acylation and predict the final product
b-draw the major resonance contributor of the sigma complex formed in the first acylation

0 0
Add a comment Improve this question Transcribed image text
Answer #1

I HOPE ITS HELPFUL TO YOU..IF YOU HAVE ANY DOUBTS PLS COMMENTS BELOW..I WILL BE THERE TO HELP YOU..ALL THE BEST...

Appointments Knoan a 10 AlCl3 に orea 14 CI-Alcl 15 I C CI 17 Impertant Calls JUNE 2015 Cals to Reply S 16 17 19 20 2222 25

I HOPE ITS HELPFUL TO YOU..PLS RATE THUMBS UP...ITS HELPS ME ALOT....

THANK YOU.....!!

Add a comment
Know the answer?
Add Answer to:
ketone products can be efficiently constructed by sequential Friedal-Crafts acylations with phosgene. a- draw an arrow...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • VI. Mechanism. (14) 1. Draw a stepwise electron pushing mechanism to predict the products in the...

    VI. Mechanism. (14) 1. Draw a stepwise electron pushing mechanism to predict the products in the following reduction. Make sure to show the correct locations of any deuterium (D) labels (4) 1. LA EXCESS) Co che le 2 0,09 2. Draw a complete stepwise electron pushing mechanism for the acylation of toluene below. Make sure to clearly indicate the role of the catalyst and how it is regenerated. Also clearly indicate why the methyl substituent directs the cyl group to...

  • сн, Нас 12-addition products (direct addition) CH2 CH3 Н,с Н-с CH CI HCI CH2 Cн Н.с 1,4-addition products (conjuga...

    сн, Нас 12-addition products (direct addition) CH2 CH3 Н,с Н-с CH CI HCI CH2 Cн Н.с 1,4-addition products (conjugate addition) Cн CH3 Нас Н.С CI Electrophilic addition to an alkene proceeds via Markovnikov regiochemistry due to the formation of the more stable carbocation intermediate. In the case of conjugated dienes, that is dienes that are separated by one sigma bond, the carbocation that is formed is stabilized additionally by resonance. Addition of the nucleophile to the carbocation intermediate can therefore...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT